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Poly(ADP-ribose) polymerase-1 polymorphisms, expression and activity in selected human tumour cell lines
BACKGROUND: Poly(ADP-ribose) polymerase-1 (PARP-1) is a DNA-binding enzyme activated by DNA breaks and involved in DNA repair and other cellular processes. Poly(ADP-ribose) polymerase activity can be higher in cancer than in adjacent normal tissue, but cancer predisposition is reported to be greater...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2720202/ https://www.ncbi.nlm.nih.gov/pubmed/19568233 http://dx.doi.org/10.1038/sj.bjc.6605166 |
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author | Zaremba, T Ketzer, P Cole, M Coulthard, S Plummer, E R Curtin, N J |
author_facet | Zaremba, T Ketzer, P Cole, M Coulthard, S Plummer, E R Curtin, N J |
author_sort | Zaremba, T |
collection | PubMed |
description | BACKGROUND: Poly(ADP-ribose) polymerase-1 (PARP-1) is a DNA-binding enzyme activated by DNA breaks and involved in DNA repair and other cellular processes. Poly(ADP-ribose) polymerase activity can be higher in cancer than in adjacent normal tissue, but cancer predisposition is reported to be greater in individuals with a single-nucleotide polymorphism (SNP) V762A (T2444C) in the catalytic domain that reduces PARP-1 activity. METHODS: To resolve these divergent observations, we determined PARP-1 polymorphisms, PARP-1 protein expression and activity in a panel of 19 solid and haematological, adult and paediatric human cancer cell lines. RESULTS: There was a wide variation in PARP activity in the cell line panel (coefficient of variation, CV=103%), with the lowest and the highest activity being 2460 pmol PAR/10(6) (HS-5 cells) and 85 750 pmol PAR/10(6) (NGP cells). Lower variation (CV=32%) was observed in PARP-1 protein expression with the lowest expression being 2.0 ng μg(−1) (HS-5 cells) and the highest being 7.1 ng μg(−1) (ML-1 cells). The mean activity in the cancer cells was 45-fold higher than the mean activity in normal human lymphocytes and the PARP-1 protein levels were 23-fold higher. CONCLUSIONS: Surprisingly, there was no significant correlation between PARP activity and PARP-1 protein level or the investigated polymorphisms, T2444C and CA. |
format | Text |
id | pubmed-2720202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-27202022010-07-21 Poly(ADP-ribose) polymerase-1 polymorphisms, expression and activity in selected human tumour cell lines Zaremba, T Ketzer, P Cole, M Coulthard, S Plummer, E R Curtin, N J Br J Cancer Translational Therapeutics BACKGROUND: Poly(ADP-ribose) polymerase-1 (PARP-1) is a DNA-binding enzyme activated by DNA breaks and involved in DNA repair and other cellular processes. Poly(ADP-ribose) polymerase activity can be higher in cancer than in adjacent normal tissue, but cancer predisposition is reported to be greater in individuals with a single-nucleotide polymorphism (SNP) V762A (T2444C) in the catalytic domain that reduces PARP-1 activity. METHODS: To resolve these divergent observations, we determined PARP-1 polymorphisms, PARP-1 protein expression and activity in a panel of 19 solid and haematological, adult and paediatric human cancer cell lines. RESULTS: There was a wide variation in PARP activity in the cell line panel (coefficient of variation, CV=103%), with the lowest and the highest activity being 2460 pmol PAR/10(6) (HS-5 cells) and 85 750 pmol PAR/10(6) (NGP cells). Lower variation (CV=32%) was observed in PARP-1 protein expression with the lowest expression being 2.0 ng μg(−1) (HS-5 cells) and the highest being 7.1 ng μg(−1) (ML-1 cells). The mean activity in the cancer cells was 45-fold higher than the mean activity in normal human lymphocytes and the PARP-1 protein levels were 23-fold higher. CONCLUSIONS: Surprisingly, there was no significant correlation between PARP activity and PARP-1 protein level or the investigated polymorphisms, T2444C and CA. Nature Publishing Group 2009-07-21 2009-06-30 /pmc/articles/PMC2720202/ /pubmed/19568233 http://dx.doi.org/10.1038/sj.bjc.6605166 Text en Copyright © 2009 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Translational Therapeutics Zaremba, T Ketzer, P Cole, M Coulthard, S Plummer, E R Curtin, N J Poly(ADP-ribose) polymerase-1 polymorphisms, expression and activity in selected human tumour cell lines |
title | Poly(ADP-ribose) polymerase-1 polymorphisms, expression and activity in selected human tumour cell lines |
title_full | Poly(ADP-ribose) polymerase-1 polymorphisms, expression and activity in selected human tumour cell lines |
title_fullStr | Poly(ADP-ribose) polymerase-1 polymorphisms, expression and activity in selected human tumour cell lines |
title_full_unstemmed | Poly(ADP-ribose) polymerase-1 polymorphisms, expression and activity in selected human tumour cell lines |
title_short | Poly(ADP-ribose) polymerase-1 polymorphisms, expression and activity in selected human tumour cell lines |
title_sort | poly(adp-ribose) polymerase-1 polymorphisms, expression and activity in selected human tumour cell lines |
topic | Translational Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2720202/ https://www.ncbi.nlm.nih.gov/pubmed/19568233 http://dx.doi.org/10.1038/sj.bjc.6605166 |
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